Linked Data
gnomAD v4:
11-67482980-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67482980C>T , CM000673.2:g.67482980C>T | GRCh38 |
| NC_000011.9:g.67250451C>T , CM000673.1:g.67250451C>T | GRCh37 |
| NC_000011.8:g.67007027C>T | NCBI36 |
| NG_008969.1:g.4947C>T , LRG_460:g.4947C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682699.1:c.-179C>T | ENSP00000507935.1:n.-179C>T | |
| XM_024448761.1:c.-179C>T | XP_024304529.1:n.-179C>T |